Pregnancy Clinical Trial
— Bump2BeOfficial title:
Blood Glucose Training for Women With Type 1 Diabetes Contemplating Pregnancy
Verified date | October 2016 |
Source | University of Virginia |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
Ineffective management of blood glucose (BG) levels during preconception and pregnancy has
been associated with severe maternal and fetal complications in women with type 1 diabetes
(T1DM). Preconception care emphasizing stringent glycemic control in the preconception
period and continued through early pregnancy can dramatically reduce these risks. However,
the use of preconception care in the US has been disappointingly low due to a variety of
organizational, provider, and patient centered factors. Furthermore, efforts to achieve
tight glycemic control can increase the risk of severe hypoglycemia (SH) in T1DM women,
potentially leading to serious health consequences. In this project, the investigators will
test an education based Internet intervention (Bump2be or Blood glucose awareness training
(BGAT) for users who might become pregnant) for use with T1DM women who are either actively
trying to become pregnant (TP) or planning to become pregnant in the 12 months following
their enrollment in this study (PP).
The main objective is to examine Bump2be's feasibility and preliminary efficacy as an
intervention for these women to better regulate their BG levels and to meet their
diabetes-related clinical targets for pregnancy. More specifically, Bump2be will be tested
in a randomized clinical trial in which 58 T1DM women who are either TP or PP will be
recruited. As part of this pre-post study design, participants will be randomly assigned to
either the Bump2be intervention (n=29) or the routine care group (n=29). Data collected will
include frequency of extreme BG, consequences of extreme BG, average BG levels (HbA1c
level), estimation of BG, detection of low and high BG, and psychological functioning
(including fear of hypoglycemia, avoidance of hyperglycemia, well-being, and internal locus
of control). Interviews with up to 10 trial participants will be conducted at the conclusion
of their study participation, to enable further optimization of the intervention in
preparation for a subsequent R01 submission. This will be the first study investigating the
use of the Internet to improve detection and management of extreme BG levels in Diabetes
mellitus type 1 (T1DM) women who are either TP or PP.
Status | Completed |
Enrollment | 54 |
Est. completion date | October 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion Criteria: - Must be diagnosed with T1DM for at least a year - Either actively trying to get pregnant or planning to become pregnant in the 12 months following enrollment in this study - Own and routinely use a BG memory meter - Measure BG more than twice per day - Should be able to download personal BG meter onto a computer - Be able to read and speak English - Be able to provide informed consent - Have regular access to a computer and the Internet, and be able to view the website content independently - Reside in the United States Exclusion Criteria: - Residents of another country - Unable to travel to Lab Corp for blood work |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
United States | University of Viginia Center for Behavioral Health & Technology | Charlottesville | Virginia |
Lead Sponsor | Collaborator |
---|---|
University of Virginia | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
Cox D, Ritterband L, Magee J, Clarke W, Gonder-Frederick L. Blood glucose awareness training delivered over the internet. Diabetes Care. 2008 Aug;31(8):1527-8. doi: 10.2337/dc07-1956. Epub 2008 May 13. — View Citation
Singh H, Murphy HR, Hendrieckx C, Ritterband L, Speight J. The challenges and future considerations regarding pregnancy-related outcomes in women with pre-existing diabetes. Curr Diab Rep. 2013 Dec;13(6):869-76. doi: 10.1007/s11892-013-0417-5. Review. — View Citation
Singh H, Owen S, Crook M, Gonder--Frederick L, Ingersoll & Ritterband L (2014) Women's experiences of pregnancy in type 1 diabetes: Implications for patient care. Annals of Behavioral Medicine, 47(Supplement 1): s17, A---054.
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduced frequency of extreme BG (as defined by the low and high BG index) | 3 months (during the intervention period) | No | |
Primary | Reduced consequences of extreme BG (e.g., diabetic ketoacidosis, SH) | 3 months (during the intervention period) | No | |
Secondary | Improved estimation of BG (as confirmed by BG Diary data) | 3 months (during the intervention period) | No | |
Secondary | Improved detection of low and high BG (as confirmed by BG Diary data) | 3 months (during the intervention period) | No | |
Secondary | Reduced fear of hypoglycemia (as confirmed by the Low Blood Sugar Survey) | Assessed pre and post intervention | No | |
Secondary | Reduced extreme avoidance of hyperglycemia (as confirmed by the High Blood Sugar Survey) | Assessed pre and post intervention | No | |
Secondary | Improved well-being (as confirmed by the Diabetes Distress Scale) | Assessed pre and post intervention | No | |
Secondary | Improved internal locus of control (as confirmed by the Perceived Competence for Diabetes Scale and the Treatment Self-Regulation Questionnaire) | Assessed pre and post intervention | No |
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